DrugJul 16, 2025
KABANA SKIN CARE GreenScreen, kabana organic skincare, Bread Spectrum UVA & UVB, Zinc Oxide recall — FDA D-0514-2025
cGMP deviations
Class IIFDA: OngoingKABANA SKIN CARE
Monthly breakdown
2025 recalls by month
Select a month to review the recall records reported during that period.
December 2025389 records · 4 categoriesNovember 2025326 records · 4 categoriesOctober 2025455 records · 4 categoriesSeptember 2025285 records · 4 categoriesAugust 2025239 records · 4 categoriesJuly 2025370 records · 4 categoriesJune 2025342 records · 4 categoriesMay 2025258 records · 4 categoriesApril 2025302 records · 4 categoriesMarch 2025259 records · 4 categoriesFebruary 2025260 records · 4 categoriesJanuary 2025354 records · 4 categories
2025 recalls — page 78
Records are ordered by the best available source date.
VehicleJul 11, 2025
Ford fuel injection system recall — NHTSA campaign 25V467000
Ford Motor Company (Ford) is recalling certain 2021-2024 Bronco Sport and 2020-2022 Escape vehicles equipped with 1.5L engines. A fuel injector may crack and leak fuel inside the engine…
fuel injection systemFord Motor Company
Medical DeviceJul 9, 2025
Siemens Healthcare Diagnostics ADVIA 120/2120/2120i SETpoint Calibrator recall — FDA Z-2086-2025
Products have the incorrect platelet (PLT) value assignments for the ADVIA 120/2120/2120i Hematology Systems.
Class IIFDA: OngoingSiemens Healthcare Diagnostics, Inc.
Medical DeviceJul 9, 2025
Philips S7-3t Transducer recall — FDA Z-2060-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
Geneoscopy ColoSense Test Kit, Part No. 80-001, component of ColoSense test recall — FDA Z-2077-2025
Multiple plate failures documented as a result of the Low Positive Template Control being too high and out of range using the affected lot of ColoSense Test Kit.
Class IIFDA: OngoingGeneoscopy, Inc.
Medical DeviceJul 9, 2025
VITROS 5600 Integrated System recall — FDA Z-2038-2025
A software anomaly allows test results to be reported using Micro Tip and Micro Slide diluent packs that the system treats as expired even when the Use Expired Reagents setting is not…
Class IIFDA: OngoingOrtho-Clinical Diagnostics, Inc.
Medical DeviceJul 9, 2025
Medline convenience kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 recall — FDA Z-2045-2025
Medline Industries, LP. is issuing a recall for specific Medline kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN which was identified that during insertion of the…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceJul 9, 2025
Philips L9-3 Transducer recall — FDA Z-2057-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
VITROS 4600 Chemistry System recall — FDA Z-2040-2025
a software anomaly allows test results to be reported using Micro Tip and Micro Slide diluent packs that the system treats as expired even when the Use Expired Reagents setting is not…
Class IIFDA: OngoingOrtho-Clinical Diagnostics, Inc.
Medical DeviceJul 9, 2025
Siemens Medical Solutions USA ARTIS is a family of dedicated angiography systems developed recall — FDA Z-2019-2025
In very rare situations, communication between the sensor measuring dose applied to the area and the corresponding software fails. As a result of the failure, the system may incorrectly…
Class IIFDA: OngoingSiemens Medical Solutions USA, Inc.
Medical DeviceJul 9, 2025
Maquet Critical Care AB Servo-u MR Ventilator System recall — FDA Z-2015-2025
Potential for inaccurate measurement of the patient circuit compliance during the patient circuit test due to combination of incorrect pre-use leakage test and use of an incorrect active…
Class IFDA: OngoingMaquet Critical Care AB
Medical DeviceJul 9, 2025
C.R. Bard BD Heyman Follower Coude Tip for following sizes: 12Fr - REF:021312 14Fr recall — FDA Z-2075-2025
Cather packaging may contain the incorrect French size.
Class IIFDA: OngoingC.R. Bard Inc.
Medical DeviceJul 9, 2025
Philips L8-4 Transducer recall — FDA Z-2056-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
Philips VL13-5 Transducer recall — FDA Z-2063-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
Siemens Healthcare Diagnostics ADVIA 120/2120/2120i 3-in-1 TESTpoint Control (ABN1 Control) recall — FDA Z-2087-2025
Products have the incorrect platelet (PLT) value assignments for the ADVIA 120/2120/2120i Hematology Systems.
Class IIFDA: OngoingSiemens Healthcare Diagnostics, Inc.
Medical DeviceJul 9, 2025
Becton, Dickinson and Company, BD Bio Sciences REF: 335775 , BD FACS, 7-Color Setup Beads recall — FDA Z-2078-2025
Due to customer complaints, errors in spectral overlap factors table for 7-color setup beads may affect accurate setup of the flow cytometry instrument prior to analyzing samples.
Class IIFDA: OngoingBecton, Dickinson and Company, BD Bio Sciences
Medical DeviceJul 9, 2025
Hardy Diagnostics HardyCHROM CRE, selective and differential culture medium for recall — FDA Z-2041-2025
Identified lots failed incoming quality control testing. Lots exhibited breakthrough growth of Klebsiella pneumoniae.
Class IIFDA: OngoingHardy Diagnostics
Medical DeviceJul 9, 2025
Medline convenience kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 recall — FDA Z-2044-2025
Medline Industries, LP. is issuing a recall for specific Medline kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN which was identified that during insertion of the…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceJul 9, 2025
Philips Respironics BiPAP A30 Ventilators recall — FDA Z-2036-2025
This device does not indicate for use in patients with respiratory failure.
Class IFDA: OngoingPhilips Respironics, Inc.
Medical DeviceJul 9, 2025
Change Healthcare Cardiology Hemo Software recall — FDA Z-2071-2025
Due to complaints, software update may cause software to unexpectedly shutdown.
Class IIFDA: OngoingCHANGE HEALTHCARE CANADA COMPANY
Medical DeviceJul 9, 2025
Maquet Critical Care AB Servo-n Ventilator System recall — FDA Z-2014-2025
Potential for inaccurate measurement of the patient circuit compliance during the patient circuit test due to combination of incorrect pre-use leakage test and use of an incorrect active…
Class IFDA: OngoingMaquet Critical Care AB
Medical DeviceJul 9, 2025
Philips L12-4 Transducer recall — FDA Z-2055-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
C.R. Bard BD Heyman Follower Straight Tip for following sizes: 10Fr - REF:21110, 12Fr recall — FDA Z-2074-2025
Cather packaging may contain the incorrect French size.
Class IIFDA: OngoingC.R. Bard Inc.
Medical DeviceJul 9, 2025
Philips C5-1 Transducer recall — FDA Z-2049-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
About the 2025 recall archive
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.